Sr. Automation Engineer - Upstream/Media Novartis - 4.1 Durham, NC Job Details Full-time $108,500 - $201,500 a year 1 day ago Benefits Health insurance 401(k) matching Qualifications Content creation for technical audiences Project management experience in technology Technical documentation Pharmaceutical regulatory compliance Technical writing experience within manufacturing Equipment troubleshooting

FDA 21 CFR

Part 11 GMP Project management experience in manufacturing Pharmaceutical company experience Supervisory control and data acquisition (SCADA) Managing projects Pharmaceutical manufacturing facility experience Production troubleshooting Full Job Description Summary Ready to help power the next generation of life-changing therapies? As a Sr. Automation Engineer - Upstream/Media, you will play a critical role in supporting the automation systems that drive upstream manufacturing and media preparation operations. You'll serve as a technical leader within a GMP environment, partnering with cross-functional teams to optimize process performance, enhance system reliability, and deliver automation solutions that enable consistent, compliant production. This is an exciting opportunity to combine technical expertise, innovation, and project leadership while helping shape the future of advanced biopharmaceutical manufacturing. About the

Role Location:

This position will be located in Durham, NC and will be an onsite role. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

Lead automation support for upstream manufacturing and media process control systems. Serve as the technical SME for DCS, BMS, MES, and associated control systems. Drive automation project execution from concept through implementation and operational handoff. Oversee integration of third-party equipment into site automation and manufacturing platforms. Develop URS, FS, and design specifications to support compliant system delivery. Collaborate with cross-functional teams to establish priorities, timelines, and project objectives. Support new product introductions and upstream process implementation within GMP manufacturing. Investigate automation-related non-conformances and implement effective corrective actions. Execute change controls, system upgrades, and continuous improvement initiatives. Provide technical support for manufacturing operations, including participation in on-call rotations.

Essential Requirements:

Bachelor's degree in Engineering, Computer Science, or a related technical discipline. 8+ years of automation experience within GMP pharmaceutical or biopharmaceutical manufacturing environments. Hands-on experience supporting DCS platforms, preferably Emerson DeltaV. Proven expertise with PLC, SCADA, HMI, and manufacturing automation systems. Strong knowledge of validation practices, GMP regulations, FDA requirements, and 21 CFR Part 11. Experience applying ISA-88 principles and developing automation standards within regulated environments. Demonstrated project leadership experience, including management of contractors and external partners. Strong troubleshooting, communication, and technical writing skills with the ability to solve complex challenges.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $108,500 and $201,500 annually The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. #

LI-Onsite Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?

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Benefits and Rewards:

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EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility & Reasonable Accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Division Operations Business Unit Information Technology Location USA State North Carolina Site Durham Company / Legal Entity U061 (FCRS = US061) Novartis Services, Inc. Functional Area Technical Operations Job Type Full time Employment Type Regular Shift Work No